MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2032487
rs2032487
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE MYH9 SNPs rs4821480, rs2032487, rs4281481 and rs3752462 are associated with T2DM-ESRD susceptibility in European Americans. 21968013 2012
dbSNP: rs3752462
rs3752462
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE MYH9 SNPs rs4821480, rs2032487, rs4281481 and rs3752462 are associated with T2DM-ESRD susceptibility in European Americans. 21968013 2012
dbSNP: rs11089788
rs11089788
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Based on a large Chinese IgAN cohort, we found an association between rs11089788 and prognosis of IgAN, adding to the mounting evidence of MYH9 as an important gene in IgAN to ESRD. 21245129 2011
dbSNP: rs2413396
rs2413396
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Four single neucleotide polymorphisms (SNPs) (rs3752462, rs4821480, rs11089788 and rs2413396) reported to be associated with ESRD with the most significance were genotyped by TaqMan assay or a restriction fragment length polymorphism assay for a further case-control study. 21245129 2011
dbSNP: rs4821480
rs4821480
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.010 GeneticVariation BEFREE Four single neucleotide polymorphisms (SNPs) (rs3752462, rs4821480, rs11089788 and rs2413396) reported to be associated with ESRD with the most significance were genotyped by TaqMan assay or a restriction fragment length polymorphism assay for a further case-control study. 21245129 2011